L-Glutamate Antibody – Mouse Monoclonal

Ref: IS018
ICCIFIHCNeuromediatorsMonoclonal Antibodies
DatasheetMSDS

Anti-L-Glutamate antibody IS018 is a mouse monoclonal Ab specifically selected by competitive ELISA for its affinity and specificity features. Using with the STAINperfect immunostaining kit A, our antibody directly labels L-Glutamate in whole mounts, cell culture and tissue sections.

Clonality Monoclonal antibody
Host Mouse
Applications IHCIF
Reactivity Reacts with all species
Tested samples whole mounts, cell culture, tissue sections
Staining procedure STAINperfect immunostaining kit A
Format 50 µL
References Cited 1 paper
Size

50µL

From: 449.00

STAINperfect™ immunostaining kit A

76 in stock

Quantity
Total

449.00

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Product overview


Product name L-Glutamate antibody – mouse mAb
Synonyms Anti-L-Glutamic acid antibody
Immunogen Conjugated L-Glutamate
Specificity When tested in competitive ELISA, the anti-conjugated Glutamate antibody did not show any significant cross reactivity with its analogs, including D-Glutamate
Clone 1D51B1
Volume 50 µL

 

Storage


Form Liquid
Purity Purified IgG
Storage Store at +4°C for short term (1-2 months). Aliquot and store at -20°C for long term. Avoid repeated freeze / thaw cycles
Material safety datasheet Download MSDS

IF – Cell cultures, Whole mounts, Tissue sections Dilute antibody with the antibody diluent provided in the STAINperfect immunostaining kit A. Use at 1/250 -1/1000 dilution. Follow the STAINperfect protocol suited to your sample
Comments Optimal working dilutions must be determined by the end-user
Restrictions For research use only
Full protocol Download STAINperfect protocol for L-Glutamate staining
Protocols-at-a-glance
Complete
Instructions for Use
Protocol-at-a-glance
for cell cultures
Protocol-at-a-glance
for whole mounts
Protocol-at-a-glance
for tissue sections

Product citations

  • Impact of Sleep-Wake-Associated Neuromodulators and Repetitive Low-Frequency Stimulation on Human iPSC-Derived Neurons
    Check the article
    Authors : Yokoi et al., Frontiers in neuroscience
    2019-05

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